Canonical Allele Identifier: PA645485708
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 336667
ClinVar RCV Id: RCV000594107 RCV000882202 RCV001081489 RCV004549765
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Val119Ile
CA1673288
NM_002618.4:c.355G>A